Potency of gastrointestinal colonization and virulence of Candida auris in a murine endogenous candidiasis

PLoS One. 2020 Dec 2;15(12):e0243223. doi: 10.1371/journal.pone.0243223. eCollection 2020.

Abstract

Background: Candida auris infections have recently emerged worldwide, and this species is highly capable of colonization and is associated with high levels of mortality. However, strain-dependent differences in colonization capabilities and virulence have not yet been reported.

Objectives: In the present study, we aimed to clarify the differences between clinically isolated invasive and non-invasive strains of C. auris.

Methods: We evaluated colonization, dissemination, and survival rates in wild C57BL/6J mice inoculated with invasive or non-invasive strains of C. auris under cortisone acetate immunosuppression, comparing with those of Candida albicans and Candida glabrata infections. We also evaluated the potency of biofilm formation.

Results: Stool fungal burdens were significantly higher in mice inoculated with the invasive strains than in those infected with the non-invasive strain. Along with intestinal colonization, liver and kidney fungal burdens were also significantly higher in mice inoculated with the invasive strains. In addition, histopathological findings revealed greater dissemination and colonization of the invasive strains. Regarding biofilm-forming capability, the invasive strain of C. auris exhibited a significantly higher capacity of producing biofilms. Moreover, inoculation with the invasive strains resulted in significantly greater loss of body weight than that noted following infection with the non-invasive strain.

Conclusions: Invasive strains showed higher colonization capability and rates of dissemination from gastrointestinal tracts under cortisone acetate immunosuppression than non-invasive strains, although the mortality rates caused by C. auris were lower than those caused by C. albicans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biofilms / growth & development
  • Candida / pathogenicity
  • Candida / physiology*
  • Candida albicans / pathogenicity
  • Candida albicans / physiology
  • Candida glabrata / pathogenicity
  • Candida glabrata / physiology
  • Candidiasis / microbiology
  • Candidiasis / pathology*
  • Candidiasis, Invasive / microbiology
  • Candidiasis, Invasive / pathology*
  • Gastrointestinal Tract / microbiology*
  • Gastrointestinal Tract / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Virulence

Supplementary concepts

  • Candida auris infection

Grants and funding

This work was supported in part by the Research Program on Emerging and Re-emerging Infectious Diseases of the Japan Agency for Medical Research and Development (AMED) under Grant Number (JP19fk0108045, JP19fk0108049, JP19fk0108094, and JP19fk0108104), and by JSPS KAKENHI Grant Number JP17K10040. JP19fk0108045, JP19fk0108049, JP19fk0108094, and JP17K10040 were given to YM. JP19fk0108104 was given to HK and HH. URL of AMED is https://www.amed.go.jp/en/index.html URL of JSPS KAKENHI is https://www.jsps.go.jp/english/index.html The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.